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ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEF) CASE INVESTIGATION FORM AEF Form 3 EPIDEMIOLOGY UNIT, MINISTRY OF HEALTH The MOH should do the investigation personally. Necessary data should be obtained
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How to fill out aefi case investigation form

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How to fill out an AEFI case investigation form:

01
Start by carefully reading and understanding the instructions provided on the form. Familiarize yourself with the purpose of the form and the information required.
02
Begin filling out the personal details section of the form. This typically includes the patient's name, age, gender, contact information, and any relevant medical history.
03
Move on to the section where you describe the adverse event. Provide a detailed account of the symptoms experienced by the patient, including the date and time of onset, severity, duration, and any other pertinent information.
04
Include information about the vaccine received by the patient, including the name, manufacturer, batch number, and the date it was administered.
05
Describe any medical treatment that was provided to the patient after the adverse event occurred. Include details about the healthcare professional who administered the treatment, the medications or therapies given, and the outcome of the treatment.
06
If applicable, mention any laboratory tests or diagnostic procedures that were conducted to investigate the adverse event. Include the details of the tests performed, the results obtained, and the interpretation of those results.
07
Discuss any previous vaccinations or adverse events experienced by the patient. Provide details about the vaccines received, including the names, dates, and any associated adverse reactions.
08
Write down any relevant information about the patient's medical history, including pre-existing conditions or allergies. This may help in understanding the context and potential contributing factors to the adverse event.
09
In the final section, provide your contact information and any additional comments or observations you deem relevant to the case.

Who needs an AEFI case investigation form?

01
Healthcare professionals responsible for administering vaccines should complete the AEFI case investigation form when an adverse event following immunization occurs. This could include doctors, nurses, or other medical practitioners.
02
Public health officials and researchers may also utilize the AEFI case investigation form to monitor and analyze adverse events associated with immunization. This data helps to ensure the safety and effectiveness of vaccines.
03
Vaccine manufacturers and regulatory authorities may require the completion of an AEFI case investigation form to accurately record and investigate any adverse events reported in relation to their vaccines.
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The AEFI case investigation form is a document used to gather detailed information about adverse events following immunization.
Healthcare providers and stakeholders involved in immunization programs are required to file AEFI case investigation forms.
The AEFI case investigation form must be completed by healthcare providers with precise and detailed information about the adverse event following immunization.
The purpose of the AEFI case investigation form is to investigate and document adverse events following immunization to ensure patient safety and improve immunization programs.
Information such as patient demographics, vaccine details, immunization history, adverse event details, and healthcare provider information must be reported on the AEFI case investigation form.
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